GATA4, GATA binding protein 4, 2626

N. diseases: 336; N. variants: 72
Disease: Atrial septal defect 2 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1842778
Disease: Atrial septal defect 2
Atrial septal defect 2 		0.900 GeneticVariation disease UNIPROT Disease Model of GATA4 Mutation Reveals Transcription Factor Cooperativity in Human Cardiogenesis. 27984724 2016
CUI: C1842778
Disease: Atrial septal defect 2
Atrial septal defect 2 		0.900 Biomarker disease MGD Congenital heart disease-causing Gata4 mutation displays functional deficits in vivo. 22589735 2012
CUI: C1842778
Disease: Atrial septal defect 2
Atrial septal defect 2 		0.900 GeneticVariation disease UNIPROT A novel mutation in GATA4 gene associated with dominant inherited familial atrial septal defect. 20347099 2010
CUI: C1842778
Disease: Atrial septal defect 2
Atrial septal defect 2 		0.900 GeneticVariation disease UNIPROT A novel mutation of GATA4 in a familial atrial septal defect. 20659440 2010
CUI: C1842778
Disease: Atrial septal defect 2
Atrial septal defect 2 		0.900 Biomarker disease GENOMICS_ENGLAND GATA4 sequence variants in patients with congenital heart disease. 18055909 2007
CUI: C1842778
Disease: Atrial septal defect 2
Atrial septal defect 2 		0.900 GeneticVariation disease UNIPROT GATA4 sequence variants in patients with congenital heart disease. 18055909 2007
CUI: C1842778
Disease: Atrial septal defect 2
Atrial septal defect 2 		0.900 GeneticVariation disease UNIPROT Spectrum of heart disease associated with murine and human GATA4 mutation. 17643447 2007
CUI: C1842778
Disease: Atrial septal defect 2
Atrial septal defect 2 		0.900 GeneticVariation disease UNIPROT Phenotypes with GATA4 or NKX2.5 mutations in familial atrial septal defect. 15810002 2005
CUI: C1842778
Disease: Atrial septal defect 2
Atrial septal defect 2 		0.900 GeneticVariation disease UNIPROT GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5. 12845333 2003
CUI: C1842778
Disease: Atrial septal defect 2
Atrial septal defect 2 		0.900 GeneticVariation disease CLINVAR
CUI: C1842778
Disease: Atrial septal defect 2
Atrial septal defect 2 		0.900 Biomarker disease GENOMICS_ENGLAND
CUI: C1842778
Disease: Atrial septal defect 2
Atrial septal defect 2 		0.900 CausalMutation disease CLINVAR
CUI: C1842778
Disease: Atrial septal defect 2
Atrial septal defect 2 		0.900 Biomarker disease CTD_human